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New · posted Oct 14

Medline · Medical Devices

Spec QA

  • Mundelein, IL
  • On-site
  • Full-time
  • Associate & Specialist
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EmploymentFull-time
Deadline

Open until filled

The role

This role specializes in one or two particular subsection(s) of our Quality Management System (e.g. Device Master Records, customer complaint, product hold, recalls, incoming quality). Responsible for basic building and maintaining quality documentation and processes such as product specifications, manufacturing tolerances, engineering drawings, inspection criteria, testing reports, ERP system analysis, customer complaint analysis and validations.

What you need

Education

  • Typically requires a Bachelor’s degree in Engineering, Science, Math or other related field.

Certification / Licensure

  • None

Work Experience

  • At least 2 years of experience in Quality.

Knowledge / Skills / Abilities

  • Experience developing ways of accomplishing goals, with little or no supervision, depending on oneself to complete objectives, and determining when escalation of issues is necessary.
  • Experience using time management skills to prioritize, organize, and track details in order to meet deadlines of multiple projects.
  • Experience using MS Office Suite products (Word, Excel, PowerPoint, Outlook ), with an Intermediate skill in Excel.
  • Experience in processing all relevant details, understanding and prioritizing their importance, and drawing clear and concise conclusions.
  • Working knowledge of government and industry quality assurance standards (e.g. 21 CFR 820, ISO 13485).
  • Position requires up to 10% travel

Knowledge / Skills / Abilities

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.

The anticipated salary range for this position:

$67,000.00 - $101,000.00 Annual

The actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.

We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.

What you'll do

  1. Assist in the development and implementation of processes, reports, data analysis and procedures within the defined area of specialization.
  2. Collaborate with multiple groups (both internal and external) to solve complex problems and continue to ensure compliance is maintained with FDA, ISO and internal requirements.
  3. Facilitate meetings with global business units, sales, marketing, branch personnel to manage project requirements and deadlines. Track and report progress periodically to management.
  4. Review all related documentation and analysis for completeness, accuracy, and assure the product and reports meets all specifications.
  5. Make recommendations and decisions based off the documentation and analysis that leads to better quality standards and customer experience.

Pay and benefits

$67,000 – $101,000 a year

Employer provided
How this compares
  • Health insurance

  • Life and disability insurance

  • 401(k) contributions

  • Paid time off

  • Bonus/incentive eligible

  • Continuing education & training

Where you'll work

Mundelein, ILOn-siteOpen in Maps (opens in a new tab)

More jobs in Mundelein, IL
Equal opportunity, accessibility and legal noticesMedline's statements, word for word

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

Job intelligence

The context around this role

Live data · October 14, 2026

Salary intelligence

How the pay compares

This role's midpoint is 5% above the US median for Quality Assurance roles at this level.

This roleEmployer provided

$67,000 to $101,000 a year

Associate & Specialist roles in Illinois18 roles publishing pay

Middle half $84,000 to $99,000, median $99,000

Associate & Specialist roles in the US111 roles publishing pay

Middle half $71,250 to $99,000, median $80,000
Annual base pay
Annual base payLowMedianHigh
This role$67,000—$101,000
Illinois$84,000$99,000$99,000
All US$71,250$80,000$99,000

This role: Medline's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 14, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Assurance

The general path across 598 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Medline's own promotion track.

  1. This role

    Associate & Specialist

    Often: Quality Engineer · Intern

    $80K median156 open
  2. Next step

    Senior & Principal

    Often: Quality Engineer · Supplier Quality Engineer

    $125K median269 open
  3. Later

    Manager

    Often: Manager, Quality Assurance · QA Supervisor

    $156K median92 open
  4. Later

    Director

    Often: Associate Director · Associate Director, GMP Operational Quality

    $211K median69 open
  5. Later

    VP & Executive

    Often: AVP · Executive Director Quality, Cell & Gene Therapy

    $293K median12 open

Skills DNA

What this role leans on

How many of the posting's 21 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 3 linesLab testing and methods: 1 lineDocumentation and SOPs: 5 linesInvestigations and CAPA: 1 lineValidation and qualification: 1 lineQuality systems and risk: 2 linesData and digital systems: 1 lineCollaboration and leadership: 4 linesGMPLab testingDocumentationInvestigationsValidationQuality systemsData systemsTeamwork
  • Documentation and SOPs5
  • Collaboration and leadership4
  • GMP and compliance3
  • Quality systems and risk2
  • Lab testing and methods1
  • Investigations and CAPA1
  • Validation and qualification1
  • Data and digital systems1

Company hiring pulse

Medline on Regulatory Jobs

46
Open roles
36
Distinct roles
20
Locations

By discipline

  • Quality41 89%
  • Regulatory5 11%

By level

  • Associate & Specialist28 61%
  • Senior & Principal11 24%
  • Director3 7%
See all 46 Medline roles

More roles at Medline

All 46 Medline roles

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Spec QA at Medline

Open until filled. $67K–$101K a year, employer provided.

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    Spec QA at Medline — Mundelein, IL | Regulatory Jobs